Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 9 de 9
Filtrar
1.
J Card Surg ; 37(12): 4816-4824, 2022 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-36413694

RESUMEN

BACKGROUND: The most worrisome complications in patients supported by left ventricular assist device (LVAD) are pump thrombosis, embolism, and bleeding. The actual rate of these events in patients with sickle-cell disease (SCD) has not well investigated. The aim of our study is to evaluate the outcomes of LVAD implantation in patients with sickle-cell hemoglobinopathy at our institution. METHODS: This retrospective, observational, single-center study was conducted on patients with sickle-cell trait (SCT), who underwent LVAD implantation using the HeartMate3 LVAD. RESULTS: LVAD devices were implanted in four patients with SCT. All procedures were performed successfully. All patients had uneventful post-implant course. Overall, the mean follow-up time was 25 months (range 21-28 months) and showed an unremarkable post-implant course. There was a significant improvement in hematological markers over the follow-up period. CONCLUSIONS: Despite the limited numbers of patients enrolled in this study, our findings indicate that LVAD surgery is safe in SCD patients and offers remarkable clinical improvement. Further studies are needed to provide more evidence regarding this type of patients undergoing LVAD implantation.


Asunto(s)
Anemia de Células Falciformes , Insuficiencia Cardíaca , Trasplante de Corazón , Corazón Auxiliar , Trombosis , Humanos , Estudios Retrospectivos , Insuficiencia Cardíaca/cirugía , Trombosis/etiología , Anemia de Células Falciformes/complicaciones , Anemia de Células Falciformes/terapia , Corazón Auxiliar/efectos adversos
2.
Artif Organs ; 46(7): 1429-1435, 2022 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-35554959

RESUMEN

OBJECTIVES: To highlight the role of percutaneous left ventricular assist device (LVAD) decommissioning as a safe procedure after myocardial recovery in patients with advanced heart failure. BACKGROUND: The HeartMate3 LVAD (Abbott, Chicago, IL, USA) is designed to provide circulatory support with enhanced hemocompatibility for patients with advanced heart failure. Most VADs are used as a bridge to heart transplantation; however, in certain cases, myocardial function recovers, and VADs can be explanted after the patient is weaned. Although surgical explantation remains the gold standard, minimally invasive percutaneous decommissioning has been described as a successful alternative. In this study, we present our experience, one-year outcomes, and adverse events associated with percutaneous LVAD decommissioning. METHODS: We conducted a retrospective review of data from six consecutive patients who underwent percutaneous LVAD decommissioning. RESULTS: Six patients were enrolled in the study. For all six patients, HM3 decommissioning was completed at least 6 months ago. No technical complications were documented. No strokes were observed within the study period, and the ejection fraction improved. The mean follow-up duration was 18 ± 8.5 months, and the survival rate was 100%. CONCLUSION: Percutaneous HeartMate3 decommissioning appears to be safe. In particular, the survival after the procedure was 100%, and no events, especially thromboembolic ones, occurred.


Asunto(s)
Insuficiencia Cardíaca , Trasplante de Corazón , Corazón Auxiliar , Remoción de Dispositivos/métodos , Insuficiencia Cardíaca/cirugía , Corazón Auxiliar/efectos adversos , Humanos , Estudios Retrospectivos , Resultado del Tratamiento , Función Ventricular Izquierda
3.
J Craniofac Surg ; 32(6): e572-e578, 2021 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-34054093

RESUMEN

ABSTRACT: Severely atrophic alveolar ridges represent a great challenge for implant-prosthetic rehabilitations. The aim of this study was to clinically and histologically evaluate horizontal and vertical bone gain, as well as implant survival/success rate after guided bone regeneration (GBR) for the reconstruction of large bone defects. Fourteen subjects (7 males and 7 females; mean age: 48.9 ±â€Š14.1) were enrolled in the study. They were selected according to specific inclusion criteria and all patients required GBR procedures for placing implants in severe atrophic jaws (bone height ≤6 mm). Guided bone regeneration was performed using dense polytetrafluoroethylene nonresorbable titanium-reinforced membranes associated with particulate heterologous bone grafts. Implant placement was performed 6 months after surgery at the same time as the removal of the membrane. Furthermore, a biopsy sample from the grafted sites was collected to conduct a histological analysis of the regenerated bone. Forty-seven dental implants were placed and followed up after prosthetic loading. Seventeen sites, 8 in the maxilla and 9 in the mandible, were suitable for the GBR procedure. The healing period was uneventful in 13 sites. The average value of vertical bone regeneration was 5.88 ±â€Š1.17 mm. Postloading follow-up ranged from 24 to 59 months. During the follow-up, clinical and radiographic exams showed no significant bone resorption and, in each case, the criteria for implants' survival were respected with no signs of any complications. Histological analysis of the bone biopsy samples revealed residual graft particulate in close contact with newly formed bone. Guided bone regeneration is a reliable technique for reconstruction of severe atrophic ridges. Larger long-term follow-up studies are needed to evaluate the condition of the bone grafted over time and its ability to support functional loading of the implants.


Asunto(s)
Aumento de la Cresta Alveolar , Implantes Dentales , Adulto , Proceso Alveolar , Atrofia , Regeneración Ósea , Trasplante Óseo , Implantación Dental Endoósea , Femenino , Regeneración Tisular Guiada Periodontal , Humanos , Masculino , Persona de Mediana Edad , Estudios Retrospectivos , Resultado del Tratamiento
4.
Am J Cardiol ; 138: 66-71, 2021 01 01.
Artículo en Inglés | MEDLINE | ID: mdl-33065081

RESUMEN

Permanent pacemaker implantation (PPI) represents a rare complication after cardiac surgery, with no uniform agreement on timing and no information on follow-up. A multicenter retrospective study was designed to assess pacemaker dependency (PMD) and long-term mortality after cardiac surgery procedures. Between 2004 and 2016, PPI-patients from 18 centers were followed. Time-to-event data were evaluated with semiparametric regression Cox models and semiparametric Fine and Gray model for competing risk framework. Of 859 (0.90%) PPI-patients, 30% were pacemaker independent (PMI) at 6 months. PMD showed higher mortality compared with PMI (10-year survival 80.1% ± 2.6% and 92.2% +2.4%, respectively, log-rank p-value < 0.001) with an unadjusted hazard ratio for death of 0.36 (95% CI 0.20 to 0.65, p< 0.001 favoring PMI) and an adjusted hazard ratio of 0.19 (95% CI 0.08 to 0.45, p< 0.001 with PMD as reference). Crude cumulative incidence function of restored PMI rhythm at follow-up at 6 months, 1 year and 12 years were 30.5% (95% CI 27.3% to 33.7%), 33.7% (95% CI 30.4% to 36.9%) and 37.2% (95% CI 33.8% to 40.6%) respectively. PMI was favored by preoperative sinus rhythm with normal conduction (SR) (HR 2.37, 95% CI 1.65 to 3.40, p< 0.001), whereas coronary artery bypass grafting and aortic valve replacement were independently associated with PMD (HR 0.63, 95% CI 0.45 to 0.88, p = 0.006 and HR 0.807, 95% CI 0.65 to 0.99, p = 0.047 respectively). Time-to-implantation was not associated with increased rate of PMI. Although 30% of PPI-patients are PMI after 6 months, PMD is associated with higher mortality at long term.


Asunto(s)
Bloqueo Atrioventricular/epidemiología , Bradicardia/epidemiología , Estimulación Cardíaca Artificial , Procedimientos Quirúrgicos Cardíacos , Mortalidad , Marcapaso Artificial , Complicaciones Posoperatorias/epidemiología , Anciano , Anciano de 80 o más Años , Bloqueo Atrioventricular/terapia , Bradicardia/terapia , Puente de Arteria Coronaria , Femenino , Implantación de Prótesis de Válvulas Cardíacas , Humanos , Masculino , Persona de Mediana Edad , Complicaciones Posoperatorias/terapia , Modelos de Riesgos Proporcionales , Estudios Retrospectivos
5.
F1000Res ; 8: 263, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-32595936

RESUMEN

Background: The Institute for Healthcare Improvement (IHI) has proposed a new method, the Global Trigger Tool (IHI GTT), to detect and monitor adverse events (AEs) and provide information to implement improvement. In 2015, the Sicilian Health System adopted IHI GTT to assess the number, types and severity levels of AEs. The GTT was implemented in 44 of 73 Sicilian public hospitals and 18,008 clinical records (CRs) were examined. Here we present the standardized application of the GTT and the preliminary results of 14,706 reviews of CRs. Methods: IHI GTT was adapted, developed and implemented to the local context. Reviews of CRs were conducted by 199 professionals divided into 71 review teams consisting of three individuals: two of whom had clinical knowledge and expertise, and a physician to authenticate the AE. The reviewers entered data into a dedicated IT-platform. All 44 of the public hospitals were included, with approximately 300,000 yearly inpatient admissions out of a population of approximately 5 million. In total, 14,706 randomized CRs of inpatients from medicine, surgery, obstetric and ICU wards, from June 2015 to June 2018 were reviewed. Results: In 975 (6.6%) CRs at least one AE was found. Approximately 20,000 patients of the 300,000 discharged each year in Sicily have at least one AE. In 5,574 (37.9%) CRs at least one trigger was found. A total of 1,542 AEs were found. The analysis of ROC curve shows that the presence of two triggers in a CR indicates with high probability the presence of an AE. The most frequent type of AE was in-hospital related infection. Conclusions: The GTT is an efficient method to identify AEs and to track improvement of care. The analysis and monitoring of some triggers is important to prevent AEs. However, it is a labor-intensive method, particularly if the CRs are paper-based.


Asunto(s)
Seguridad del Paciente , Mejoramiento de la Calidad/organización & administración , Infección Hospitalaria/epidemiología , Implementación de Plan de Salud , Humanos , Admisión del Paciente , Alta del Paciente , Evaluación de Programas y Proyectos de Salud , Sicilia
6.
Rev. bioét. derecho ; (42): 33-49, mar. 2018.
Artículo en Italiano | IBECS | ID: ibc-170956

RESUMEN

Consumatori e istituzioni considerano l’etichetta come una sorta di bussola indispensabile ai fini dell'orientamento nell'acquisto dei prodotti alimentari. Tuttavia, le informazioni che quest'ultima include, pur essendo veritiere, non sempre lo permettono, perché le indicazioni obbligatorie, di per sé o nell'interazione con le indicazioni facoltative, con la pubblicità o con il bagaglio identitario e cognitivo dei consumatori, possono veicolare messaggi allusivi, impliciti e fuorvianti. Il presente articolo intende analizzare i processi rappresentativi e volitivi sottostanti alla scelta di acquisto, che nel caso specifico assume caratteristiche sue proprie in ragione del bene oggetto del contratto e delle condizioni in cui questo si conclude. Inoltre, si propone di indagare l'interferenza del professionista nel processo decisionale del consumatore, attraverso lo studio di alcuni casi che mettono in evidenza i limiti intrinseci dell'etichetta come strumento informativo


Both consumers and institutions consider food label as an essential compass in the purchase of foodstuffs. However, label information, although truthful, does not always allow consumer orientation. Indeed, mandatory information, either per se or in interaction with optional elements, advertising, or with the identity and cognitive baggage in consumers’ psyches, may end up providing suggestive, implicit or misleading messages. This paper aims at analyzing the representative and volitional processes underlying purchasing decisions, which - in this specific case - assume particular characteristics depending on the type of good that is the object of the contract and on the special conditions under which it is concluded. The article also seeks to investigate the interference of professionals in the decision-making process. This will be done through the study of several leading cases that highlight the intrinsic limits of the label as an informative tool


Los consumidores y las instituciones consideran la etiqueta como una especie de brújula indispensable para orientarse a la hora de adquirir los productos alimenticios. Sin embargo, a pesar de ser verdaderas, las informaciones incluidas en las etiquetas no siempre lo permiten, ya que las indicaciones obligatorias, de por sí o en interacción con las indicaciones voluntarias, con la publicidad o con el bagaje identitario y cognitivo de los consumidores, pueden transmitir mensajes alusivos, implícitos o engañosos. El presente artículo pretende analizar los procesos representativos y volitivos subyacentes a la decisión de compra, la cual, en el caso específico, adquiere características propias en razón del bien objeto del contrato y de las condiciones en las que éste termina. Además, se propone investigar la interferencia del profesional en el proceso decisional del consumidor a través del estudio de unos casos que ponen en evidencia los límites intrínsecos de la etiqueta como herramienta informativa


Els consumidors i les institucions consideren l'etiqueta com una espècie de brúixola indispensable per orientar-se a l'hora d'adquirir els productes alimentaris. No obstant això, malgrat ser veritables, les informacions incloses en les etiquetes no sempre ho permeten, ja que les indicacions obligatòries, de per si mateixes o en interacció amb les indicacions voluntàries, amb la publicitat o amb el bagatge identitari i cognitiu dels consumidors, poden transmetre missatges al·lusius, implícits o enganyosos. El present article pretén analitzar els processos representatius i volitius subjacents a la decisió de compra, la qual, en el cas específic, adquireix característiques pròpies en raó del bé objecte del contracte i de les condicions en les quals aquest acaba. A més, es proposa investigar la interferència del professional en el procés de decisió del consumidor a través de l'estudi de casos que posen en evidència els límits intrínsecs de l'etiqueta com a eina informativa


Asunto(s)
Defensa del Consumidor/tendencias , Seguridad de Productos para el Consumidor/normas , Etiquetado de Alimentos/tendencias , Fraude/tendencias , Acceso a la Información/legislación & jurisprudencia
8.
Int J Cardiol ; 241: 97-102, 2017 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-28390740

RESUMEN

BACKGROUND: The aim of this large retrospective study was to provide a logistic risk model along an additive score to predict early mortality after surgical treatment of patients with heart valve or prosthesis infective endocarditis (IE). METHODS: From 2000 to 2015, 2715 patients with native valve endocarditis (NVE) or prosthesis valve endocarditis (PVE) were operated on in 26 Italian Cardiac Surgery Centers. The relationship between early mortality and covariates was evaluated with logistic mixed effect models. Fixed effects are parameters associated with the entire population or with certain repeatable levels of experimental factors, while random effects are associated with individual experimental units (centers). RESULTS: Early mortality was 11.0% (298/2715); At mixed effect logistic regression the following variables were found associated with early mortality: age class, female gender, LVEF, preoperative shock, COPD, creatinine value above 2mg/dl, presence of abscess, number of treated valve/prosthesis (with respect to one treated valve/prosthesis) and the isolation of Staphylococcus aureus, Fungus spp., Pseudomonas Aeruginosa and other micro-organisms, while Streptococcus spp., Enterococcus spp. and other Staphylococci did not affect early mortality, as well as no micro-organisms isolation. LVEF was found linearly associated with outcomes while non-linear association between mortality and age was tested and the best model was found with a categorization into four classes (AUC=0.851). CONCLUSIONS: The following study provides a logistic risk model to predict early mortality in patients with heart valve or prosthesis infective endocarditis undergoing surgical treatment, called "The EndoSCORE".


Asunto(s)
Procedimientos Quirúrgicos Cardíacos/mortalidad , Endocarditis/diagnóstico , Endocarditis/mortalidad , Prótesis Valvulares Cardíacas , Infecciones Relacionadas con Prótesis/diagnóstico , Infecciones Relacionadas con Prótesis/mortalidad , Adulto , Anciano , Anciano de 80 o más Años , Procedimientos Quirúrgicos Cardíacos/tendencias , Femenino , Prótesis Valvulares Cardíacas/microbiología , Humanos , Modelos Logísticos , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Estudios Retrospectivos , Resultado del Tratamiento
9.
Epidemiol Prev ; 28(1): 34-40, 2004.
Artículo en Italiano | MEDLINE | ID: mdl-15148871

RESUMEN

OBJECTIVE: To compare hospital mortality in a cardiac surgery unit with external data and to assess changes in time (patients undergoing surgery in two different periods). MATERIALS AND METHODS: Data on risk factors for hospital mortality were collected from clinical records (retrospectively for the first period and prospectively for the second) for all patients undergoing open heart surgery at the Heart Surgery Unit of the University of Turin (Italy) during 1991 and 1995 (n = 1794) and 1999 (n = 892). Comparisons of in-hospital mortality, expressed as Standardized Mortality Ratios (SMR), were adjusted for risk factors defined according to EuroSCORE (European System for Cardiac Operative Risk Evaluation). RESULTS: In the first and second period, complete information on all the 17 EuroSCORE items was available for 58.3% and 89.6% patients respectively. After exclusion of patients with one or more missing data, observed and expected numbers of death were found to be very similar, with SMRs ranging between 0.82 (isolated bypass in the second period) and 1.06 ("other" surgery in the first period). Mortality was higher among patients with missing data, but at least in 1999 the latter had a limited impact on the overall estimates. Compared to the first period, mortality was reduced during 1999 (from 5.9% to 5.4%), in particular for isolated bypass (from 4.4% to 3.4%). CONCLUSIONS: In the unit under investigation, hospital mortality following heart surgery was similar to that predicted from EuroSCORE and seemed to be lower in 1999 than in 1991-95, particularly for isolated bypass. Incompleteness of data on individual risk factors may have been a source of bias, especially when data were collected retrospectively.


Asunto(s)
Procedimientos Quirúrgicos Cardíacos/mortalidad , Mortalidad Hospitalaria/tendencias , Adolescente , Adulto , Anciano , Anciano de 80 o más Años , Femenino , Salud Global , Humanos , Italia , Masculino , Persona de Mediana Edad
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA